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What is the chemical structure of (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methano-2,1-benzothiazole 2,2-dioxide?
This is the chemical structure of (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole-2,2-dioxide. The chemical structure of this compound is indeed an important research object in the field of organic chemistry. Among its structures, the specific three-dimensional configurations (S, R, R) at 3a, 6, and 7a determine the uniqueness of the molecular spatial arrangement. 8,8-dimethyl indicates that there are two methyl groups connected at a specific location in the molecule, which affects the physical and chemical properties of the molecule. The structural skeleton of hexahydro-3a, 6-methylene-2,1-benzothiazole is based on benzothiazole, and the hexahydro structure endows the molecule with different stability and reactivity. The part of 2,2-dioxide, that is, the sulfur atom at the 2nd position on the thiazole ring, is connected to the two oxygen atoms to form a dioxygen structure, which greatly changes the electron cloud distribution and polarity of the molecule. The interaction of these structural characteristics makes the compound exhibit specific chemical behavior and potential application value, and may have important uses in many fields such as medicinal chemistry and materials science.
What are the physical properties of (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methano-2,1-benzothiazole 2,2-dioxide?
(3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide, this is an organic compound. It has many physical properties.
Looking at its properties, it may be solid under normal conditions, because this class of compounds containing benzothiazole structure and multiple substituents have strong intermolecular forces, causing them to tend to be solid. Its melting point, or due to the tight accumulation of molecules and strong interaction, is in a certain temperature range. Specifically, the conjugated system of the benzene ring, the steric hindrance of the methyl group, and the methylene bridging structure in the structure synergistically affect the molecular arrangement and interaction, resulting in a relatively high melting point.
Discussing solubility, because it contains polar sulfone groups (oxides), it may have a certain solubility in polar organic solvents such as ethanol and acetone. However, there are also non-polar methyl groups and benzothiazole skeletons in the molecule, which make it limited in solubility in non-polar solvents such as n-hexane.
Looking at its density, due to the compact molecular structure and large atomic weight, the density may be higher than that of water. The presence of benzothiazole rings and multiple methyl groups increases the mass per unit volume.
As for volatility, due to its strong intermolecular forces, volatility is low. This is due to high melting point and intermolecular interactions that prevent molecules from escaping from the liquid or solid surface.
In summary, (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide The physical properties of the compound are determined by its unique molecular structure, which is of great significance for its applications in chemical, pharmaceutical and other fields.
What is the main use of (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methano-2,1-benzothiazole 2,2-dioxide?
(3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide, which is an organic compound. However, the name of this specific compound is not known in the books of "Tiangong Kaiwu". Gai "Tiangong Kaiwu" was formed in the Ming Dynasty, when chemical knowledge was very different from the fine nomenclature and cognition of today's organic compounds.
Today, (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide may have applications in the field of organic synthesis. Or it can be used as a key intermediate to participate in the construction of complex organic molecules. Through its unique chemical structure and reactivity, it can be converted into an organic compound with special functions or properties through specific chemical reactions.
In the field of medicinal chemistry, or this compound can be modified to explore its potential biological activity, such as its effect on specific disease-related targets, hoping to develop new drugs. In the field of materials science, its own structure may endow materials with unique properties, such as improving material stability, optical properties, etc., which can be applied to the preparation of specific materials. Although this substance is not covered in "Tiangong Kaiji", in the current development of science and technology, such compounds show many potential application directions.
What are the synthesis methods of (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methano-2,1-benzothiazole 2,2-dioxide?
The synthesis method of (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide is described in detail.
To prepare this product, you can first take suitable starting materials, such as benzothiazole derivatives with specific substituents. First, the derivative is reacted with a reagent that can introduce dimethyl in a suitable reaction environment, such as the presence of a specific solvent and catalyst. This reaction requires attention to the reaction temperature, time and the ratio of reactants, and precise regulation to successfully connect the dimethyl to the target position. < Br >
Then, the steps to construct the hexahydro-3a, 6-methylene structure are carried out. It is often necessary to use a specific cyclization reaction, or to use the reaction characteristics of active groups such as alkenyl and alkynyl groups, through cycloaddition and other reactions, to promote the formation of the desired hexahydro-3a, 6-methylene structure in the molecule. In this process, the polarity of the solvent and the pH of the reaction system have a great influence on the reaction process and product configuration, so careful consideration is required.
Furthermore, for the oxidation of sulfur atoms to form the dioxide structure, suitable oxidizing agents, such as m-chloroperoxybenzoic acid, can be selected. Control the amount of oxidant and reaction conditions to ensure that sulfur atoms are precisely oxidized to dioxide without affecting other sensitive groups in the molecule.
During the synthesis process, the reaction products at each step need to be analyzed and identified in detail, and the structure and purity of the products need to be confirmed by means such as nuclear magnetic resonance and mass spectrometry. In this way, through multiple delicate reactions and careful regulation, (3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide can be obtained.
(3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methano-2,1-benzothiazole 2,2-dioxide What are the precautions during use?
(3aS, 6R, 7aR) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole-2,2-dioxide When using this product, many matters need to be paid attention to.
First of all, this product has special properties. When storing, it must be in a dry, cool and well-ventilated place. Do not approach fire or heat sources to prevent its properties from mutating or causing accidents. Due to its special chemical structure, if it is not stored properly, it may cause changes in molecular structure, affect its effectiveness, and even cause dangerous changes.
Furthermore, when using, the operator must strictly abide by the operating procedures. You need to wear appropriate protective equipment, such as gloves, goggles, etc., to ensure your own safety. Because of its irritation to the skin and eyes, if you accidentally touch it, you should immediately rinse with plenty of water and seek medical attention as appropriate.
In terms of the use environment, ensure that the space is well ventilated. This substance may evaporate certain gases during use. If the ventilation is poor, the gas will accumulate, which will affect the health of the operator on the one hand, and may pose a potential danger such as explosion on the other.
At the same time, the amount used needs to be precisely controlled. Excessive use will not only fail to increase its effectiveness, but may instead cause adverse consequences, such as environmental contamination, or unexpected products in subsequent reactions. And after use, the remaining items and waste should not be discarded at will, and should be properly disposed of in accordance with relevant regulations to avoid damage to the surrounding environment. In short, when using this item, all details should not be ignored, so as to ensure safe and effective use.